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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Benzoic acid, 5-chloro-4-fluoro-2-hydroxy-

OC(=O)c1cc(Cl)c(cc1O)F Request for Quotation
Chemical Name: Benzoic acid, 5-chloro-4-fluoro-2-hydroxy-
CAS Number: 189283-52-1
Product Number: AG002I72(AGN-PC-03KMF6)
Synonyms:
MDL No:
Molecular Formula: C7H4ClFO3
Molecular Weight: 190.5563

Identification/Properties

Computed Properties
Molecular Weight:
190.554g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
189.983g/mol
Monoisotopic Mass:
189.983g/mol
Topological Polar Surface Area:
57.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
188
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Chloro-4-fluoro-2-hydroxybenzoic acid, also known as $name$, is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. In the realm of organic chemistry, this compound serves as a valuable building block for the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. One of the key applications of 5-Chloro-4-fluoro-2-hydroxybenzoic acid is its role as a precursor in the synthesis of biologically active compounds. By utilizing the functional groups present in this compound, chemists can introduce specific molecular modifications to tailor the properties of the final product. This flexibility allows for the development of novel drug candidates with improved efficacy and reduced side effects. Furthermore, 5-Chloro-4-fluoro-2-hydroxybenzoic acid can be used as a starting material for the construction of complex molecular frameworks through various chemical transformations. Its reactivity towards different reagents and reaction conditions enables the creation of diverse chemical structures, making it an indispensable tool in organic synthesis.Overall, the versatile nature of 5-Chloro-4-fluoro-2-hydroxybenzoic acid makes it a valuable asset in the arsenal of synthetic chemists, contributing to the advancement of chemical research and the development of innovative products.